Rui Xu

发表

N-Glycolylneuraminic acid deficiency worsens cardiac and skeletal muscle pathophysiology in α-sarcoglycan-deficient mice.

A. Varki, Chiou-Miin Wang, P. Janssen, 2013, Glycobiology.

rAAVrh74.MCK.GALGT2 Protects against Loss of Hemodynamic Function in the Aging mdx Mouse Heart.

Ying Jia, Paul T Martin, Rui Xu, 2019, Molecular therapy : the journal of the American Society of Gene Therapy.

Vascular delivery of rAAVrh74.MCK.GALGT2 to the gastrocnemius muscle of the rhesus macaque stimulates the expression of dystrophin and laminin α2 surrogates.

J. Mendell, C. Walker, K. Clark, 2014, Molecular therapy : the journal of the American Society of Gene Therapy.

A Comparative Study of N-glycolylneuraminic Acid (Neu5Gc) and Cytotoxic T Cell (CT) Carbohydrate Expression in Normal and Dystrophin-Deficient Dog and Human Skeletal Muscle

K. Flanigan, A. Varki, J. Kornegay, 2014, PloS one.

Deletion of Galgt2 (B4Galnt2) reduces muscle growth in response to acute injury and increases muscle inflammation and pathology in dystrophin-deficient mice.

J. Bauer, K. Chandrasekharan, Rui Xu, 2015, The American journal of pathology.

Postnatal overexpression of the CT GalNAc transferase inhibits muscular dystrophy in mdx mice without altering muscle growth or neuromuscular development: Evidence for a utrophin-independent mechanism

M. Camboni, Rui Xu, Paul T. Martin, 2007, Neuromuscular Disorders.

CB2/miR-124 signaling down-regulate the expression of purinergic P2X4 and P2X7 receptor in dorsal spinal cord of CCI rats

Zhi Xiao, Fan Yang, Rui Xu, 2020 .

Comparative proteomic profiling of dystroglycan-associated proteins in wild type, mdx, and Galgt2 transgenic mouse skeletal muscle.

F. Montanaro, Laura T Martin, J. Yoon, 2012, Journal of proteome research.

A Method to Produce and Purify Full-Length Recombinant Alpha Dystroglycan : Analysis of Nand O-Linked Monosaccharide Composition in CHO Cells with or without LARGE Overexpression

J. Yoon, Rui Xu, Paul T. Martin, 2018 .

rAAVrh74.MCK.GALGT2 Demonstrates Safety and Widespread Muscle Glycosylation after Intravenous Delivery in C57BL/6J Mice

B. Bolon, Ying Jia, J. Yoon, 2019, Molecular therapy. Methods & clinical development.

A Method to Produce and Purify Full-Length Recombinant Alpha Dystroglycan: Analysis of N- and O-Linked Monosaccharide Composition in CHO Cells with or without LARGE Overexpression

J. Yoon, Rui Xu, Paul T. Martin, 2013, PLoS currents.

Muscular dystrophy associated with α-dystroglycan deficiency in Sphynx and Devon Rex cats

E. Engvall, K. North, R. Malik, 2008, Neuromuscular Disorders.

Deletion of Pofut1 in Mouse Skeletal Myofibers Induces Muscle Aging-Related Phenotypes in cis and in trans

P. White, Ying Jia, Rui Xu, 2017, Molecular and Cellular Biology.

Intra-CA1 Administration of Minocycline Alters the Expression of Inflammation-Related Genes in Hippocampus of CCI Rats

T. Xu, Junwei Zeng, Song Cao, 2019, Front. Mol. Neurosci..

Overexpression of Galgt2 reduces dystrophic pathology in the skeletal muscles of alpha sarcoglycan-deficient mice.

M. Camboni, Rui Xu, Paul T. Martin, 2009, The American journal of pathology.

Distinct contributions of Galgt1 and Galgt2 to carbohydrate expression and function at the mouse neuromuscular junction

Rui Xu, N. Singhal, Paul T. Martin, 2012, Molecular and Cellular Neuroscience.

The synaptic CT carbohydrate modulates binding and expression of extracellular matrix proteins in skeletal muscle: Partial dependence on utrophin

J. Yoon, K. Chandrasekharan, Rui Xu, 2009, Molecular and Cellular Neuroscience.

B4GALNT2 (GALGT2) Gene Therapy Reduces Skeletal Muscle Pathology in the FKRP P448L Mouse Model of Limb Girdle Muscular Dystrophy 2I.

Rui Xu, P. Thomas, Paul T. Martin, 2016, The American journal of pathology.

Soluble Heparin Binding Epidermal Growth Factor-Like Growth Factor Is a Regulator of GALGT2 Expression and GALGT2-Dependent Muscle and Neuromuscular Phenotypes

Rui Xu, Paul T. Martin, M. Cramer, 2019, Molecular and Cellular Biology.

Overexpression of Galgt2 in skeletal muscle prevents injury resulting from eccentric contractions in both mdx and wild-type mice.

J. Mendell, K. Clark, L. Rodino‐Klapac, 2009, American journal of physiology. Cell physiology.

Overexpression of Galgt 2 in skeletal muscle prevents injury resulting from eccentric contractions in both mdx and wild-type mice

J. Mendell, K. Clark, L. Rodino‐Klapac, 2009 .

Overexpression of the cytotoxic T cell (CT) carbohydrate inhibits muscular dystrophy in the dyW mouse model of congenital muscular dystrophy 1A.

J. Yoon, K. Chandrasekharan, M. Camboni, 2007, The American journal of pathology.

Mouse Model of Limb Girdle Muscular Dystrophy 2 I

Rui Xu, P. Thomas, Paul T. Martin, 2016 .

An Isolated Limb Infusion Method Allows for Broad Distribution of rAAVrh74.MCK.GALGT2 to Leg Skeletal Muscles in the Rhesus Macaque

K. Flanigan, J. Cheatham, L. Rodino‐Klapac, 2018, Molecular therapy. Methods & clinical development.

Active and passive immunization strategies based on the SDPM1 peptide demonstrate pre-clinical efficacy in the APPswePSEN1dE9 mouse model for Alzheimer's disease

Chiou-Miin Wang, B. Kaspar, Carlos J. Miranda, 2014, Neurobiology of Disease.

RIPK1/RIPK3-Mediated Necroptosis is Involved in Sevoflurane-Induced Neonatal Neurotoxicity in the Rat Hippocampus

Rui Xu, W. Li, J. Jia, 2021, Cellular and Molecular Neurobiology.

Vascular delivery of rAAVrh74.MCK.GALGT2 to the gastrocnemius muscle of the rhesus macaque stimulates the expression of dystrophin and laminin α2 surrogates.

J. Mendell, C. Walker, L. Chicoine, 2014, Molecular therapy : the journal of the American Society of Gene Therapy.